EP1448059A2 - Saatbeizmittel - Google Patents

Saatbeizmittel

Info

Publication number
EP1448059A2
EP1448059A2 EP02803894A EP02803894A EP1448059A2 EP 1448059 A2 EP1448059 A2 EP 1448059A2 EP 02803894 A EP02803894 A EP 02803894A EP 02803894 A EP02803894 A EP 02803894A EP 1448059 A2 EP1448059 A2 EP 1448059A2
Authority
EP
European Patent Office
Prior art keywords
methyl
component
phenyl
active ingredient
propagation material
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP02803894A
Other languages
English (en)
French (fr)
Inventor
Birgit Forster
Franz Brandl
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Syngenta Participations AG
Original Assignee
Syngenta Participations AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Syngenta Participations AG filed Critical Syngenta Participations AG
Publication of EP1448059A2 publication Critical patent/EP1448059A2/de
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647Triazoles; Hydrogenated triazoles
    • A01N43/6531,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Definitions

  • the present invention relates to f ungicidal mixtures for the treatment of plant propagation material and to methods of using such mixtures in crop protection.
  • mixtures according to the invention comprise at least two fungicidally active components together with a suitable carrier material, wherein component I is
  • the fungicidal mixtures according to the invention have very advantageous properties for protecting plants against disease infestation, particularly in the control and prevention of disease infestation on seed and soil.
  • plant vigor Another property improved by the instant mixtures is summarized as plant vigor. Under the term plant vigor there are understood various sorts of improvements of plants which are not connected to the control of pests.
  • Such advantageous properties are improved crop characteristics including: emergence, crop yields, protein content, more developed root system, tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, less fertilizer needed, less seeds needed, more productive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, increased plant stand and early germination; or any other advantages familiar to a person skilled in the art.
  • Such enhancements were not to be expected from the activity of the individual components.
  • the weight ratio is selected as to give the desired, for example synergistic, action. In general, the weight ratio 1:11 is from 30:1 to 1 :30, preferably from 15:1 to 1 :15.
  • mixtures may be mixed with other pesticides, preferably fungicides, resulting in some cases in unexpected synergistic activities.
  • the active ingredient mixtures in question can be used as dressings in the treatment of plant propagation material, especially seed (fruit, tubers, grains) and plant cuttings (e.g. rice), to provide protection against fungus infections on the seed as well as against phytopathogenic fungi which occur in the soil.
  • plant propagation material especially seed (fruit, tubers, grains) and plant cuttings (e.g. rice)
  • plant cuttings e.g. rice
  • the active ingredient mixtures according to the invention are distinguished by the fact that they are especially well tolerated by plants and are environmentally friendly.
  • the active ingredient mixtures are effective against phytopathogenic fungi belonging to the following classes: Ascomycetes (e.g. Penicillium, Gaeumannomyces graminis); Basidiomycetes (e.g. the genus Hemileia, Rhizoctonia, Puccinia); Fungi imperfecti (e.g. Botrytis, Helminthosporium, Rhynchosporium, Fusarium, Septoria, Cercospora, Altemaria, Pyricularia and Pseudocercosporella herpotrichoides); Oomycetes (e.g. Phytophthora, Peronospora, Bremia, Pythium, Plasmopara).
  • Ascomycetes e.g. Penicillium, Gaeumannomyces graminis
  • Basidiomycetes e.g. the genus Hemileia, Rhizoctonia, Puccinia
  • Fungi imperfecti e.g. Botrytis,
  • Target crops for the areas of indication disclosed herein comprise within the scope of this invention e.g. the following species of plants: cereals (wheat, barley, rye, oats, corn, maize, rice, sorghum and related crops); beet (sugar beet and fodder beet); leguminous plants (beans, lentils, peas, soybeans); oil plants (rape, mustard, sunflowers,); cucumber plants (marrows, cucumbers, melons); fibre plants (cotton, flax, hemp, jute); vegetables (spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, paprika); as well as ornamentals (flowers, shrubs, broad-leaved trees and evergreens, such as conifers).
  • cereals wheat, barley, rye, oats, corn, maize, rice, sorghum and related crops
  • beet susgar beet and fodder beet
  • leguminous plants be
  • the active ingredient mixtures according to the invention are especially advantageous for the treatment of plant propagation material, especially seeds, of cotton, corn, soybeans, rice and peanuts.
  • the mixtures of compounds I and II are normally used in the form of compositions.
  • the compounds I and II can be applied to the plant propagation material to be treated either simultaneously or in succession at short interval, for example on the same day, if desired together with further carriers, surfactants or other application-promoting adjuvants customarily employed in formulation technology.
  • Suitable carriers and adjuvants can be solid or liquid and are the substances ordinarily employed in formulation technology, e.g. natural or regenerated mineral substances, solvents, dispersants, wetting agents, tackifiers, thickeners, binders or fertilizers.
  • the compounds I and II can also be applied to the seeds (coating), either by impregnating the tubers or grains with a liquid formulation of each of the active ingredients in succession, or by coating them with an already combined wet or dry formulation.
  • the compounds of the combination are used in unmodified form or, preferably, together with the adjuvants conventionally employed in formulation technology, and are therefore formulated in known manner e.g. into emulsifiable concentrates, coatable pastes, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granules, or by encapsulation in e.g. polymer substances.
  • the methods of application such as spraying, atomizing, dusting, scattering, coating or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances.
  • Advantageous rates of application of the active ingredient mixture are generally from 2 g to 60 g, preferably from 2 g to 30 g, per 100 kg of plant propagation material, especially seed.
  • Preferred rates are from 1 g to 30 g, especially preferred 1 g to 15 g, of compound I and 1 g to 30 g, especially preferred 1 g to 15 g, of compound II per 100 kg of plant propagation material, especially seed.
  • the formulations are prepared in known manner, e.g. by homogeneously mixing and/or grinding the active ingredients with extenders, e.g. solvents, solid carriers and, where appropriate, surface-active compounds (surfactants).
  • extenders e.g. solvents, solid carriers and, where appropriate, surface-active compounds (surfactants).
  • Suitable solvents are: aromatic hydrocarbons, preferably the fractions containing 8 to 12 carbon atoms, e.g. xylene mixtures or substituted naphthalenes, phthalates, such as dibutyl phthalate or dioctyl phthalate, aliphatic hydrocarbons, such as cyclohexane or paraffins, alcohols and glycols and their ethers and esters, such as ethanol, ethylene glycol, ethylene glycol monomethyl or monoethyl ether, ketones, such as cyclohexanone, strongly polar solvents, such as N-methyl-2-pyrrolidone, dimethyl sulfoxide or dimethylformamide, as well as vegetable oils or epoxidised vegetable oils, such as epoxidised coconut oil or soybean oil; or water.
  • aromatic hydrocarbons preferably the fractions containing 8 to 12 carbon atoms, e.g. xylene mixtures or substituted naphthalenes
  • the solid carriers used are normally natural mineral fillers, such as calcite, talcum, kaolin, montmorillonite or attapulgite.
  • calcite talcum
  • kaolin kaolin
  • montmorillonite attapulgite
  • highly dispersed silicic acid or highly dispersed absorbent polymers e.g., calcite, talcum, kaolin, montmorillonite or attapulgite.
  • Suitable granulated adsorptive carriers are porous types, for example pumice, broken brick, sepiolite or bentonite, and suitable nonsorbent carriers are, for example, calcite or sand.
  • pregranulated materials of inorganic or organic nature can be used, e.g. especially dolomite or pulverized plant residues.
  • suitable surface- active compounds are non-ionic, cationic and/or anionic surfactants having good emulsifying, dispersing and wetting properties.
  • surfactants will also be understood as comprising mixtures of surfactants.
  • Particularly advantageous application-promoting adjuvants are also natural or synthetic phospholipids of the cephalin and lecithin series, e.g. phosphatidylethanolamine, phos- phatidylserine, phosphatidylglycerol and lysolecithin.
  • phospholipids of the cephalin and lecithin series e.g. phosphatidylethanolamine, phos- phatidylserine, phosphatidylglycerol and lysolecithin.
  • the agrochemical compositions normally comprise 0.1 to 99 %, especially 0.1 to 95 %, compounds I and II, 99.9 to 1 %, especially 99.9 to 5 %, of a solid or liquid adjuvant and 0 to 25 %, especially 0.1 to 25 %, of a surfactant.
  • the active ingredient is thoroughly mixed with the adjuvants and the mixture is thoroughly ground in a suitable mill, affording wettable powders which can be diluted with water to give suspensions of the desired concentration.
  • Dusts a) b) c) active ingredient [l:ll 1 :6(a), 1 :2(b), 1 :10(c)] 5 % 6 % 4 %
  • Ready-for-use dusts are obtained by mixing the active ingredient with the carrier and grinding the mixture in a suitable mill. Such powders can be used for dry dressings for seed.
  • the finely ground active ingredient is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired dilution can be obtained by dilution with water.
  • plant propagation material can be treated and protected against infestation by microorganisms, by spraying, pouring or immersion.
  • a synergistic effect exists, for example, whenever the action of an active ingredient combination is greater than the sum of the actions of the individual components.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Cultivation Of Plants (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
EP02803894A 2001-11-30 2002-11-25 Saatbeizmittel Ceased EP1448059A2 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0128722 2001-11-30
GBGB0128722.6A GB0128722D0 (en) 2001-11-30 2001-11-30 Seed treatment compositions
PCT/IB2002/005232 WO2003045150A2 (en) 2001-11-30 2002-11-25 Seed treatment compositions

Publications (1)

Publication Number Publication Date
EP1448059A2 true EP1448059A2 (de) 2004-08-25

Family

ID=9926768

Family Applications (1)

Application Number Title Priority Date Filing Date
EP02803894A Ceased EP1448059A2 (de) 2001-11-30 2002-11-25 Saatbeizmittel

Country Status (11)

Country Link
US (2) US20050085389A1 (de)
EP (1) EP1448059A2 (de)
JP (2) JP2005510529A (de)
CN (2) CN1951191A (de)
AR (1) AR037597A1 (de)
AU (1) AU2002365316B2 (de)
BR (1) BR0214555A (de)
EG (1) EG23643A (de)
GB (1) GB0128722D0 (de)
WO (1) WO2003045150A2 (de)
ZA (1) ZA200403876B (de)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0128389D0 (en) * 2001-11-27 2002-01-16 Syngenta Participations Ag Seed treatment compositions
GB0128390D0 (en) * 2001-11-27 2002-01-16 Syngenta Participations Ag Seed treatment compositions
US20050164882A1 (en) * 2002-04-10 2005-07-28 Eberhard Ammermann Method for increasing the resistance of plants to the phytotoxicity of agrochemicals
AU2005321567A1 (en) * 2004-12-23 2006-07-06 Basf Aktiengesellschaft Fungicidal mixtures containing enestroburin and at least one active substance from the group of azoles
TW200744455A (en) * 2005-07-21 2007-12-16 Syngenta Participations Ag Fungicidal combinations
CN1295962C (zh) * 2005-11-08 2007-01-24 周保东 苯醚甲环唑微乳剂
CN101404881A (zh) * 2006-03-14 2009-04-08 巴斯夫欧洲公司 引发植物的病毒耐受性的方法
JP2009529565A (ja) * 2006-03-14 2009-08-20 ビーエーエスエフ ソシエタス・ヨーロピア 細菌症に対する植物の耐性を誘導する方法
WO2007110354A2 (en) * 2006-03-24 2007-10-04 Basf Se Method for combating phytopathogenic fungi
UA104411C2 (uk) * 2007-06-29 2014-02-10 Басф Се Спосіб та застосування стробілуринового фунгіциду для поліпшення проростання і/або появи і/або збільшення висоти рослин і/або довжини кореня рослин
WO2009089687A1 (fr) * 2008-01-15 2009-07-23 Guishu Luan Granulés solubles dans l'eau de kresoxim-méthyle et leur préparation
WO2009089688A1 (fr) * 2008-01-15 2009-07-23 Guishu Luan Granulés solubles dans l'eau de fipronil et leur préparation
JP5365158B2 (ja) * 2008-11-25 2013-12-11 住友化学株式会社 植物病害防除用組成物及び植物病害の防除方法
CN101485307B (zh) * 2009-02-09 2013-02-13 吉林省八达农药有限公司 一种含有丁香菌酯与三唑类杀菌剂的农用杀真菌组合物
CN101869109B (zh) * 2010-07-08 2014-05-14 江苏省绿盾植保农药实验有限公司 含有暗罗素和醚菌酯的杀菌剂
CN102057912B (zh) * 2010-12-19 2013-04-17 惠州市银农科技有限公司 一种苯醚甲环唑和嘧菌酯混配的水悬浮剂及其制备方法
CN102204544A (zh) * 2011-04-23 2011-10-05 陕西汤普森生物科技有限公司 一种含有啶氧菌酯的增效杀菌组合物
CN102669111B (zh) * 2012-05-24 2014-06-04 利民化工股份有限公司 一种苯醚甲环唑与嘧菌酯复配的悬浮剂及其制备方法
CN102696624A (zh) * 2012-06-29 2012-10-03 青岛星牌作物科学有限公司 一种含有苯醚甲环唑和醚菌酯的杀菌组合物
US9808007B2 (en) * 2012-07-26 2017-11-07 Syngenta Participations Ag Fungicidal compositions
CN102823599B (zh) * 2012-09-24 2014-04-02 天津市汉邦植物保护剂有限责任公司 一种含醚菌酯和苯醚甲环唑的杀菌组合物及应用
CN103461383B (zh) * 2013-09-11 2015-02-25 陕西省蒲城美尔果农化有限责任公司 一种杀菌剂组合物及其生产工艺
CN103798246B (zh) * 2014-01-26 2016-03-30 上海艳紫化工科技有限公司 苯醚甲环唑和嘧菌酯复配的农药悬浮剂
CN104770379A (zh) * 2015-04-24 2015-07-15 浙江世佳科技有限公司 一种含有四霉素与苯醚甲环唑的杀菌水乳剂及其制备方法
CN106719662A (zh) * 2017-01-13 2017-05-31 佛山市盈辉作物科学有限公司 包含环己磺菌胺和氨基寡糖素的杀菌组合物
CN108522517A (zh) * 2017-03-02 2018-09-14 江苏龙灯化学有限公司 一种含有啶氧菌酯与苯醚甲环唑的杀菌组合物的应用
CN109247332A (zh) * 2018-09-15 2019-01-22 湖南农业大学 一种含苯醚甲环唑和嘧菌酯的农药组合物及其应用
BR112021006848A2 (pt) * 2018-10-31 2021-07-13 Kumiai Chemical Industry Co., Ltd. método para o controle de doenças em cereais de grãos pequenos semente de cereais de grãos pequenos e método para suprimir danos de acamamento em cereais de grãos pequenos
CN114190385A (zh) * 2021-12-23 2022-03-18 山东贵合生物科技有限公司 一种苯甲·醚菌酯粉剂及其制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE59400216D1 (de) * 1993-09-24 1996-05-23 Basf Ag Fungizide Mischungen
AU1280095A (en) * 1993-12-27 1995-07-17 Sumitomo Chemical Company, Limited Bactericidal composition
DE59706870D1 (de) * 1996-04-26 2002-05-08 Basf Ag Fungizide mischung
DE19636686A1 (de) * 1996-09-10 1998-03-12 Basf Ag Fungizide Mischungen
FR2754424A1 (fr) * 1996-10-16 1998-04-17 Rhone Poulenc Agrochimie Composition fongicide synergique comprenant un compose triazole
US6875727B2 (en) * 1997-12-23 2005-04-05 Syngenta Crop Protection, Inc. Use of macrolides in pest control
US6559136B1 (en) * 1998-11-20 2003-05-06 Bayer Aktiengesellschaft Fungicidal active substance combinations
GB0128389D0 (en) * 2001-11-27 2002-01-16 Syngenta Participations Ag Seed treatment compositions
GB0128390D0 (en) * 2001-11-27 2002-01-16 Syngenta Participations Ag Seed treatment compositions

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
None *
See also references of WO03045150A3 *

Also Published As

Publication number Publication date
AU2002365316B2 (en) 2006-07-06
CN1951191A (zh) 2007-04-25
WO2003045150A3 (en) 2004-06-10
WO2003045150A2 (en) 2003-06-05
US20050085389A1 (en) 2005-04-21
US20090325802A1 (en) 2009-12-31
JP2009221226A (ja) 2009-10-01
BR0214555A (pt) 2004-11-09
AR037597A1 (es) 2004-11-17
CN1610503A (zh) 2005-04-27
ZA200403876B (en) 2005-04-06
JP2005510529A (ja) 2005-04-21
GB0128722D0 (en) 2002-01-23
EG23643A (en) 2007-03-13
AU2002365316A1 (en) 2003-06-10

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